Senior Clinical Project Manager

Employer
Kintec Recruitment
Location
Seattle, Washington State
Salary
Competitive
Start date
17 Nov 2022
Closing date
17 Dec 2022

View more

Discipline
Clinical Research, Clinical Project Manager
Hours
Full Time
Contract Type
Permanent
Experience Level
Senior Management
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Job Details

ROLE: SENIOR CLINICAL PROJECT MANAGER

ASSIGNMENT TYPE: PERMANENT HIRE

LOCATION: SEATTLE, WASHINGTON STATE

ORGANSATION: BIOTECH COMPANY WHICH SPECIALIZES IN THE DEVELOPMENT OF ANTICANCER DRUGS

 

Kintec are partnered with a growing Biotechnology company based in Seattle, Washington State who are currently looking for a Senior Clinical Project Manager to work on a permanent hire long term basis.

 

As a Senior Clinical Project Manager, you will be responsible for the oversight of day-to-day operations for assigned studies while working closely with the contract research organization and other vendors to ensure successful study completion.

 

In your role as Senior Clinical Project Manager, you will report to the CEO but will also work closely with members of the clinical operations team, along team members from medical, pharmacology, non-clinical, CMC, business development and beyond to advance each assigned program.

 

Essential Functions

  • Responsible for the oversight of day-to-day study operations for assigned projects under the Project Director, working closely with the CRO and other selected vendors for the assigned project(s)
  • Provide Project Directors with project status updates, data, and reports as applicable and requested
  • Assist with program-level strategy, timelines, trial design, and implementation (as applicable)
  • Accountable for developing and managing project-level plans, timelines, and site budgets
  • Manage, facilitate and document project team meetings (e.g. meeting agenda, minutes, operational risk, action items and decision logs) to enable effective decision making
  • Manage study team communications to ensure cross-functional connectivity among study team members and supporting functional staff
  • Review, provide input and guide completion of CRO study related plans (i.e. project management plan, communication plan, monitoring plan, reg submission plans, training plans, risk mitigation plans, study close out plans, etc.)
  • Evaluate work processes on an ongoing basis to identify inefficiencies and gaps and provide solutions to resolve identified issues.
  • In partnership with other functional areas, participate and provide feedback to other plans (data management, medical monitoring/safety management plan, etc.); participate in UAT of systems as needed

Qualifications

  • Experience working with small Biotechnology companies
  • Experience "owning" all aspects of various projects - serving as the primary POC for internal and external parties, setting timelines and deliverables, developing and managing project budgets, leading cross-functional groups, managing vendors, etc.
  • Experience with Phase 2-3 Clinical trials
  • Experience with oncology studies preferred

This is an exciting opportunity for an experienced Senior Clinical Project Manager to partner with a growing Biotechnology company.

  • Notes
  • Perm Fee (%)

    0.00%

    Salary

    0.00

  • Internal Description

    ROLE: SENIOR CLINICAL PROJECT MANAGER

    ASSIGNMENT TYPE: PERMANENT HIRE

    LOCATION: SEATTLE, WASHINGTON STATE

    ORGANSATION: BIOTECH COMPANY WHICH SPECIALIZES IN THE DEVELOPMENT OF ANTICANCER DRUGS

     

    Kintec are partnered with a growing Biotechnology company based in Seattle, Washington State who are currently looking for a Senior Clinical Project Manager to work on a permanent hire long term basis.

     

    As a Senior Clinical Project Manager, you will be responsible for the oversight of day-to-day operations for assigned studies while working closely with the contract research organization and other vendors to ensure successful study completion.

     

    In your role as Senior Clinical Project Manager, you will report to the CEO but will also work closely with members of the clinical operations team, along team members from medical, pharmacology, non-clinical, CMC, business development and beyond to advance each assigned program.

     

    Essential Functions

    • Responsible for the oversight of day-to-day study operations for assigned projects under the Project Director, working closely with the CRO and other selected vendors for the assigned project(s)
    • Provide Project Directors with project status updates, data, and reports as applicable and requested
    • Assist with program-level strategy, timelines, trial design, and implementation (as applicable)
    • Accountable for developing and managing project-level plans, timelines, and site budgets
    • Manage, facilitate and document project team meetings (e.g. meeting agenda, minutes, operational risk, action items and decision logs) to enable effective decision making
    • Manage study team communications to ensure cross-functional connectivity among study team members and supporting functional staff
    • Review, provide input and guide completion of CRO study related plans (i.e. project management plan, communication plan, monitoring plan, reg submission plans, training plans, risk mitigation plans, study close out plans, etc.)
    • Evaluate work processes on an ongoing basis to identify inefficiencies and gaps and provide solutions to resolve identified issues.
    • In partnership with other functional areas, participate and provide feedback to other plans (data management, medical monitoring/safety management plan, etc.); participate in UAT of systems as needed

    Qualifications

    • Experience working with small Biotechnology companies
    • Experience "owning" all aspects of various projects - serving as the primary POC for internal and external parties, setting timelines and deliverables, developing and managing project budgets, leading cross-functional groups, managing vendors, etc.
    • Experience with Phase 2-3 Clinical trials
    • Experience with oncology studies preferred

    This is an exciting opportunity for an experienced Senior Clinical Project Manager to partner with a growing Biotechnology company.

Company

Established in 2001 in the United Kingdom, Kintec Global Recruitment were initially setup to service the UK’s Pharmaceutical Industry with specialist Technical & Engineering personnel. Now Kintec boast a global office network with offices in the USA, Europe, Middle East and APAC region. We provide both contingency and permanent hire recruitment solutions to CRO’s, Biotechs, Pharmaceutical & Medical Device organisations worldwide.

 

Kintec prides itself on delivering unparalleled levels of mobilisation support, which includes the organisation of visas, travel, accommodation, local payroll, security and medical insurance.

Find Us
Website
Location
4 Exchange Quay
Floor 5
Salford Quays
M5 3EE
GB

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